All diseases

OMIM ID
160120
OMIM term:
EPISODIC ATAXIA, TYPE 1; EA1
Alternative terms:
EPISODIC ATAXIA WITH MYOKYMIA; EAM
ATAXIA, EPISODIC, WITH MYOKYMIA; AEM; AEMK
PAROXYSMAL ATAXIA WITH NEUROMYOTONIA, HEREDITARY
MYOKYMIA WITH PERIODIC ATAXIA MYOKYMIA 1, INCLUDED
CONTINUOUS MUSCLE FIBER ACTIVITY, HEREDITARY, INCLUDED
ISAACS-MERTENS SYNDROME, INCLUDED
MYOKYMIA 1 WITH OR WITHOUT HYPOMAGNESEMIA, INCLUDED
(∗) Location:
12p13.32  
(†) Associated OMIM genes:
KCNA1  
(‡) Associated MGI genes:
Kcna1  

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